Inventor · disambiguated record
Imran Saeedul Haque
Also filed as: HAQUE IMRAN · HAQUE IMRAN S · HAQUE IMRAN SAEEDUL
23 granted patents·18 pending applications·105 citations·filing 2011–2025
95Inventor score
Files withMYRIAD WOMENS HEALTH INC23RECURSION PHARMACEUTICALS INC8FREENOME HOLDINGS INC6COUNSYL INC3HAQUE IMRAN1
Top patents by PatentIndex Score
41 records- 0196US12351880B2Methods of detecting and enriching circulating tumor DNAMYRIAD WOMENS HEALTH INC·Filed 2025·Granted Jul 8, 2025·2 cites·30 claims
- 0296US11932910B2Combinatorial DNA screeningMYRIAD WOMENS HEALTH INC·Filed 2021·Granted Mar 19, 2024·20 cites·14 claims
- 0395US12351879B2Enrichment of circulating tumor DNAMYRIAD WOMENS HEALTH INC·Filed 2024·Granted Jul 8, 2025·2 cites·20 claims
- 0495US12024749B2Combinatorial DNA screeningMYRIAD WOMENS HEALTH INC·Filed 2020·Granted Jul 2, 2024·8 cites·18 claims
- 0595US10597717B2Combinatorial DNA screeningMYRIAD WOMENS HEALTH INC·Filed 2017·Granted Mar 24, 2020·33 cites·11 claims
- 0694US12215392B2Methods of preparing a DNA fraction enriched with circulating tumor DNAMYRIAD WOMENS HEALTH INC·Filed 2024·Granted Feb 4, 2025·2 cites·23 claims
- 0794US12104212B2Personalized methods for detecting circulating tumor DNAMYRIAD WOMENS HEALTH INC·Filed 2023·Granted Oct 1, 2024·2 cites·18 claims
- 0894US11847532B2Machine learning implementation for multi-analyte assay development and testingFREENOME HOLDINGS INC·Filed 2021·Granted Dec 19, 2023·10 cites·7 claims
- 0993US12270082B2Methods of detecting DNA in a sampleMYRIAD WOMENS HEALTH INC·Filed 2022·Granted Apr 8, 2025·2 cites·13 claims
- 1092US11681953B2Machine learning implementation for multi-analyte assay development and testingFREENOME HOLDINGS INC·Filed 2019·Granted Jun 20, 2023·15 cites·18 claims
- 1190US2025122580A1Combinatorial dna screeningMYRIAD WOMENS HEALTH INC·Filed 2024·Application pending·0 cites
- 1290US2025066862A1Laboratory execution and automation systemsMYRIAD WOMENS HEALTH INC·Filed 2024·Application pending·0 cites
- 1388US2024150846A1Combinatorial dna screeningMYRIAD WOMENS HEALTH INC·Filed 2024·Application pending·0 cites
- 1487US12215391B1Automated methods of detecting cell free DNAMYRIAD WOMENS HEALTH INC·Filed 2023·Granted Feb 4, 2025·0 cites·16 claims
- 1585US2025095784A1Automated nucleic acid repeat count calling methodsMYRIAD WOMENS HEALTH INC·Filed 2024·Application pending·0 cites
- 1684US2025095392A1Utilizing machine learning and digital embedding processes to generate digital maps of biology and user interfaces for evaluating map efficacyRECURSION PHARMACEUTICALS INC·Filed 2024·Application pending·0 cites
- 1784US2025095146A1Utilizing machine learning and digital embedding processes to generate digital maps of biology and user interfaces for evaluating map efficacyRECURSION PHARMACEUTICALS INC·Filed 2024·Application pending·0 cites
- 1883US12344901B2Automated methods of detecting cell free DNAMYRIAD WOMENS HEALTH INC·Filed 2022·Granted Jul 1, 2025·0 cites·15 claims
- 1983US12073638B1Utilizing machine learning and digital embedding processes to generate digital maps of biology and user interfaces for evaluating map efficacyRECURSION PHARMACEUTICALS INC·Filed 2023·Granted Aug 27, 2024·0 cites·20 claims
- 2082US12079992B1Utilizing machine learning and digital embedding processes to generate digital maps of biology and user interfaces for evaluating map efficacyRECURSION PHARMACEUTICALS INC·Filed 2023·Granted Sep 3, 2024·0 cites·20 claims
- 2179US11361438B2Techniques for analyzing and detecting executional artifacts in microwell platesRECURSION PHARMACEUTICALS INC·Filed 2020·Granted Jun 14, 2022·2 cites·20 claims
- 2279US2024363195A1Systems and methods for inferring genetic ancestry from low-coverage genomic dataMYRIAD WOMENS HEALTH INC·Filed 2024·Application pending·0 cites
- 2376US10497463B2Automated nucleic acid repeat count calling methodsMYRIAD WOMENS HEALTH INC·Filed 2014·Granted Dec 3, 2019·0 cites·32 claims
- 2476US8706427B2Method for rapidly approximating similaritiesHAQUE IMRAN·Filed 2011·Granted Apr 22, 2014·7 cites·22 claims
- 2574US2024202603A1Machine learning implementation for multi-analyte assay development and testingFREENOME HOLDINGS INC·Filed 2023·Application pending·0 cites
- 2673US12033722B2Systems and methods for inferring genetic ancestry from low-coverage genomic dataMYRIAD WOMENS HEALTH INC·Filed 2022·Granted Jul 9, 2024·0 cites·20 claims
- 2772US2023175058A1Methods and systems for abnormality detection in the patterns of nucleic acidsFREENOME HOLDINGS INC·Filed 2023·Application pending·0 cites
- 2871US12080383B2Automated nucleic acid repeat count calling methodsMYRIAD WOMENS HEALTH INC·Filed 2019·Granted Sep 3, 2024·0 cites·21 claims
- 2968US2024194293A1Noninvasive prenatal screening using dynamic iterative depth optimizationMYRIAD WOMENS HEALTH INC·Filed 2023·Application pending·0 cites
- 3063US11527304B2Systems and methods for inferring genetic ancestry from low-coverage genomic dataMYRIAD WOMENS HEALTH INC·Filed 2019·Granted Dec 13, 2022·0 cites·21 claims
- 3163US2021010076A1Methods and systems for abnormality detection in the patterns of nucleic acidsFREENOME HOLDINGS INC·Filed 2020·Application pending·0 cites
- 3257US12416047B2Noninvasive prenatal diagnostic methodsMYRIAD WOMENS HEALTH INC·Filed 2017·Granted Sep 16, 2025·0 cites·31 claims
- 3357US2022238181A1Crispr guide selectionRECURSION PHARMACEUTICALS INC·Filed 2022·Application pending·0 cites
- 3455US2025218538A1Utilizing machine learning and digital embedding processes to generate digital maps of biology and user interfaces for evaluating map efficacyRECURSION PHARMACEUTICALS INC·Filed 2025·Application pending·0 cites
- 3552US11708574B2Nucleic acid sequencing adapters and uses thereofMYRIAD WOMENS HEALTH INC·Filed 2017·Granted Jul 25, 2023·0 cites·19 claims
- 3650US11854666B2Noninvasive prenatal screening using dynamic iterative depth optimizationMYRIAD WOMENS HEALTH INC·Filed 2017·Granted Dec 26, 2023·0 cites·12 claims
- 3748US2021057046A1Methods and systems for analyzing microbiotaFREENOME HOLDINGS INC·Filed 2020·Application pending·0 cites
- 3835US2016371431A1Methods of predicting pathogenicity of genetic sequence variantsCOUNSYL INC·Filed 2016·Application pending·0 cites
- 3935US2022027795A1Techniques for training a classifier to detect executional artifacts in microwell platesRECURSION PHARMACEUTICALS INC·Filed 2020·Application pending·0 cites
- 4032US2017298436A1Group testing approach for a genetic screening assayCOUNSYL INC·Filed 2017·Application pending·0 cites
- 4131US2016140289A1Variant callerCOUNSYL INC·Filed 2015·Application pending·0 cites
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Identity basis: PatentsView inventor disambiguation (2025Q4-odp release). How scoring works →